Thermoresponsive recording sheet

Description

[0001] This invention relates to a thermoresponsive recording paper sheet. More particularly, the invention relates to a thermoresponsive recording paper sheet comprising a colorless or pale-colored chromogenic substance in combination with a phenolic compound, characterized in that the thermoresponsive recording layer thereof further contains benzyl 4-benzyloxybenzoate.

[0002] It has long been known that colorless or pale-colored chromogenic substances, such as crystal violet lactone, and phenolic compounds can react to produce a color, and the use of such reaction in thermoresponsive paper sheet recording is disclosed in U.S. Patent No. 3,539,375, for instance.

[0003] However, to meet the demands for higher thermal sensitivity and high-speed responsiveness, for instance, arising from recent advances in recording devices and diversified use of thermoresponsive recording sheets, it is still necessary to solve various problems. For instance, for use on thermal printers or thermal facsimile telegraphs, thermoresponsive paper sheets should have improved thermal responsiveness in color production, since an insufficient degree of responsiveness would result in increased electric power consumption and/or decreased printing velocity. For increasing color-producing responsiveness of thermoresponsive sheets, there has already been proposed the use of such additives as waxes (Japanese Patent Application laid open (Kokai) under No. 19,231/1973), nitrogen-containing compounds (Japanese Kokai 34,842/1974) and acetoacetanilide (Japanese Kokai 106,746/1977), among others.

[0004] In thermoresponsive recording sheets, presumably a chromogenic substance and a phenolic compound are present each in the stable and finely divided state dispersedly in the same layer or in different layers and, when heated, at least one of the two components melts or both give an eutectic mixture, whereby they come into intimate contact with each other to produce a color.

[0005] U.S. Patent No. 3,539,375 describes as a phenolic compound adequate for such purpose 4,4'-isopropylidenediphenol (m.p. 156°C), which is used today in many cases. However, a considerably high temperature (e.g. 140-150⁰C) is required for distinct color production as a result of its melting. To cope with the development of high-speed recording devices as mentioned above, those thermoresponsive recording sheets with improved responsiveness which are capable of responding to a lower temperature (e.g. 80-120°C) to produce a distinct color are desired. The use of the above-mentioned waxes and so on is poor in practicability since they are water-soluble or the chromogenic substance and/or phenolic compound is scarcely soluble in them.

[0006] As a result of intensive research to improve the responsiveness in color production while removing the above-mentioned drawbacks, the present inventors have found a practicable and widely applicable method of improving said responsiveness. In accordance with the present which has now been completed, benzyl 4-benzyloxybenzoate is used as an additive in the thermoresponsive layer containing at least one colorless or pale-colored chromogenic substance and at least one phenolic compound combinedly.

[0007] The "chromogenic substance" as used herein means a compound capable of producing a color upon reaction with a phenolic compound and includes, among others, crystal violet lactone, malachite green lactone, 3,3 - bis(p - dimethylaminophenyl) - 4,5,6,7 - tetrachlorophthalide, benzo - β - naphthospiropyran, 3 - methyl - di - β - naphthospiropyran, 1,3,3 - trimethyl - 6' - chloro - 8' - methoxyindolinobenzospiropyran, N - phenylrhodamine lactam, 3 - ethylamino - 6 - chlorofluoran, 3 - morpholino - 5,6 - benzofluoran, 3 - diethylamino - 6 - methyl - 7 - anilinofluoran, 3 - diethylamino - 6 - methyl - 7 - chlorofluoran, 3 - diethylamino - 6,7 - dimethylfluoran, 3 - dimethylamino - 7,8 - benzofluoran, 3 - diethylamino - 7 - dibenzylaminofluoran, 3 - diethylamino - 7 - anilinofluoran, 3 - diethylamino - 5,6 - benzo - 7 - benzylaminofluoran, 3 - piperidino - 6 - methyl - 7 - anilinofluoran, 3 - pyrrolidino. - 6 - methyl - 7 - anilinofluoran, 3 - N - ethyl - N - tolylamino - 6 - methyl - 7 - anilinofluoran and 3 -diethylamino - -7 N - (3 -trifluoromethylphenyl)aminofluoran, but is not limited to these.

[0008] The phenolic compound should melt generally at 70°C or above and thereby react with the above-mentioned colorless or pale-colored chromogenic substance to produce a color and includes, but is not limited to, 4 - phenylphenol, 4 - methyl - 2,6 - di - tert - butylphenol, 4,4 - dihydroxydiphenyl, 4,4' - isopropylidenediphenol, 4,4' - isopropylidenebis(2 - chlorophenol), 4,4' - isopropylidenebis(2 - methylphenol), 4,4' - isopropylidenebis(2-tert-butylphenol), 4,4' - isopropylidenebis(2,6 - dimethylphenol), 4,4' - sec - butylidenediphenol, 4,4' - cyclohexylidenediphenol, 4,4' - cyclohexylidenebis(2 - methylphenol), 4,4' - cyclohexylidenebis(2 - isopropylphenol), 2,2' - methylenebis(4 - chlorophenol), 2,2' - methylenebis(4 - methyl - 6 - tert - butylphenol), 2,2 - bis(4 - hydroxyphenyl)hexane, 2,2 - bis(4 - hydroxyphenyl)heptane, 2,2 - bis(4 - hydroxyphenyl)octane, 4,4' - thiodiphenol, 4,4' - thiobis(3 - methyl - 6 - tert - butylphenol), methyl 4 - hydroxybenzoate, ethyl 4 - hydroxybenzoate, benzyl 4 - hydroxybenzoate, tolylmethyl 4 - hydroxybenzoate, phenethyl 4 - hydroxybenzoate, 3 - phenylpropyl 4 - hydroxybenzoate, phenyl 4 - hydroxybenzoate, 4 - hydroxyacetophenone, 4 - hydroxybenzophenone and salicylanilide. Benzyl 4 - benzyloxybenzoate is used, for example in an amount of 0.01 to 1 part by weight per part by weight of such phenolic compound.

[0009] In addition to benzyl 4 - benzyloxybenzoate, stearamide may be used combinedly therewith.

[0010] The thermoresponsive recording paper sheet in accordance with the present invention can be prepared by comminuting the chromogenic substance, the phenolic compound and benzyl 4-benzyloxybenzoate, each singiy or in combination of benzyl 4-benzyloxybenzoate with the chromogenic substance and/or with the phenolic compound, together with a surfactant and/or binder in water, for example in a ball mill or sand grinder and coating a paper sheet with the resulting aqueous dispersions by a conventional method, followed by drying.

[0011] The following examples iilustrate the present invention in more detail. "Part(s)" means "part(s) by weight."

[0012] In each of the above examples, Dispersions A and B were prepared separately (i.e. without mixing Dispersion A with Dispersion B) by dispersing the solid component by grinding in a ball mill for 2 days and then combined to give a coating composition for making a thermoresponsive recording paper sheet. A sheet of fine quality paper having the basis weight of 50 g/m² was coated on one side with the coating composition to the coat amount of 4 g/m² (on the dried basis) and dried at 50°C in a drier. The thermoresponsive paper sheet thus obtained was caused to produce a color by pressing the sheet against a plate heated at 80-150⁰C under the pressure of 1.5 kg/cm² (gauge) for 5 seconds. The intensity of color was measured with a photoelectric densitometer. The results obtained are shown diagrammatically in Fig. 1 in the accompanying drawing. In Fig. 1, curve (1) is for the thermoresponsive sheet of Comparative Example, curve (2) for that of Example 1 and curve (3) for that of Example 2.

Example 3

[0013] In Dispersions B in Example 1 and Example 2, the proportion of benzyl 4-benzyloxybenzoate to the phenolic compound was varied as specified below in Table 1 while the total amount of the two components was retained, and thermoresponsive recording paper sheets were prepared in the same manner as in Examples 1 and 2.

[0014] Compound A: Benzyl 4-benzyloxybenzoate (m.p. 116°C)

Phenol I: 4,4'-Isopropylidenediphenol

Phenol II: Benzyl 4-hydroxybenzoate

Phenol III: Phenethyl 4_-hydroxybenzoate

[0015] When recording was carried out on a thermal printer, the thermoresponsive recording sheets Nos. 1-9 produced distinct images with good dynamic responsiveness.

Example 4

[0016] 

Example 5

[0017] 

[0018] Using Dispersions A and B of Example 4 or 5, thermoresponsive recording paper sheets were prepared in the same manner as in Examples 1 and 2. The sheets, when recording was performed by means of a thermal printer, gave distinct images with good light resistance at high degrees of dynamic responsiveness.

Claims

1. A thermoresponsive recording paper sheet comprising a normally colorless or pale-colored chromogenic substance in combination with a phenolic compound, which comprises benzyl 4-benzyloxybenzoate as a responsiveness-increasing agent.

2. A thermoresponsive recording paper sheet according to Claim 1, wherein the phenolic compound is 4,4' -isopropylidenediphenol.

3. A thermoresponsive recording paper sheet according to Claim 1, wherein the phenolic compound is benzyl 4-hydroxybenzoate.

4. A thermoresponsive recording paper sheet according to Claim 1, wherein the chromogenic substance is a fluoran compound.

5. A thermoresponsive recording paper sheet according to Claim 4, wherein the fluoran compound is 3-diethylamino-6-methyl-7-aniiinofluoran.

6. A thermoresponsive recording paper sheet according to Claim 1, wherein the chromogenic substance is crystal violet lactone.

Ansprüche

1. Auf Wärme ansprechendes Registrierpapier-Blatt, enthaltend eine normalerweise farblose oder blaß gefärbte chromogene Substanz in Kombination mit einer Phenol-Verbindung, das Benzyl-4-benzyloxy- benzoat als die Ansprechempfindlichkeit steigerndes Mittel enthält.

2. Auf Wärme ansprechendes Registrierpapier-Blatt nach Anspruch 1, dadurch gekennzeichnet, daß die Phenol-Verbindung 4,4'-lsopropylidendiphenol ist.

3. Auf Wärme ansprechendes Registrierpapier-Blatt nach Anspruch 1, dadurch gekennzeichnet, daß die Phenol-Verbindung Benzyl-4-hydroxybenzoat ist.

4. Auf Wärme ansprechendes Registrierpapier-Blatt nach Anspruch 1, dadurch gekennzeichnet, daß die chromogene Substanz eine Fluoran-Verbindung ist.

5. Auf Wärme ansprechendes Registrierpapier-Blatt nach Anspruch 4, dadurch gekennzeichnet, daß die Fluoran-Verbindung 3-Diethylamino-6-methyl-7-anilinofluoran ist.

6. Auf Wärme ansprechendes Registrierpapier-Blatt nach Anspruch 1, dadurch gekennzeichnet, daß die chromogene Substanz Kristallviolettlacton ist.

Revendications

1. Une feuille de papier d'enregistrement thermosensible contenant une substance chromogène normalement incolore ou faiblement colorée en combinaison avec un composé phénolique, qui comprend du 4-benzyloxybenzoate de benzyle en tant qu'agent exaltant la capacité de réponse.

2. Feuille de papier d'enregistrement thermosensible selon la revendication 1, caractérisée en ce que le composé phénolique est le 4,4'-isopropylidènediphénol.

3. Feuille de papier d'enregistrement thermosensible selon la revendication 1, caractérisée en ce que le composé phénolique est le 4-hydroxybenzoate de benzyle.

4. Feuille de papier d'enregistrement thermosensible selon la revendication 1, caractérisée en ce que la substance chromogène est un composé de fluorane.

5. Feuille de papier d'enregistrement thermosensible selon la revendication 4, caractérisée en ce que le composé de fluorane est le 3-diéthylamino-6-méthyl-7-anilinofluorane.

6. Feuille de papier d'enregistrement thermosensible selon la revendication 1, caractérisée en ce que la substance chromogène est la lactone de violet cristallisé.

Drawing